RAQA Executive

Barrington James; Selangor; On-site; MYR 100,000 - 150,000; Full time

Job summary

An established industry player is seeking a dedicated RAQA Executive to ensure the highest quality standards for medical devices in the Indonesian market. This role emphasizes quality assurance and regulatory compliance, particularly for cardiovascular devices. The successful candidate will manage regulatory submissions, work with diverse teams, and stay updated on industry developments. Join a company committed to innovation and making a positive impact in healthcare, where your skills will contribute to delivering life-changing medical devices to patients in Indonesia and beyond.

Qualifications

• Proven experience in quality assurance and regulatory affairs in medical devices.
• In-depth knowledge of cardiovascular devices and local regulatory requirements.

Responsibilities

• Oversee quality assurance and regulatory affairs for medical devices in Indonesia.
• Manage regulatory submission processes and collaborate with teams.

Skills

Quality Assurance

Regulatory Affairs

Communication Skills

Problem-Solving Skills

Interpersonal Skills

Job description

Our client is a large Medical Device company with a range of commercialized products. They are committed to providing high-quality medical devices that improve the lives of patients around the world. We are dedicated to innovation, excellence, and making a positive impact in the healthcare industry. Our inclusive and diverse company culture allows us to leverage the unique talents of our employees to drive our success.

The Role

We are seeking a talented and experienced RAQA Executive to join our team and oversee the quality assurance and regulatory affairs for our medical devices in the Indonesia market. As the RAQA Executive, you will play a crucial role in ensuring that our products meet the highest standards of quality and compliance with local regulations. You will be responsible for managing the regulatory submission process, collaborating with cross-functional teams, and staying abreast of the latest developments in the industry. This role will specifically focus on cardio vascular devices such as stents and one-time use devices.

About You

• Proven experience in quality assurance and regulatory affairs within the medical device industry
• In-depth knowledge of cardio vascular devices, stents, and one-time use devices
• Strong understanding of the regulatory requirements in the Indonesia market
• Excellent communication and interpersonal skills
• Ability to work effectively in a cross-functional and multicultural environment
• Commitment to diversity, equality, and inclusion in the workplace
• Strong problem-solving skills and attention to detail

If you are passionate about making a difference in healthcare and possess the skills and experience required for this role, we would love to hear from you. Join our team at [Company Name] and contribute to our mission of delivering life-changing medical devices to patients in Indonesia and beyond.